www.smobio.com Product Information GetClone PCR Cloning Vector II CV1100 20 RXN pget II Vector (25 ng/μl) pget-for Primer (10 μm) pget-rev Primer (10 μm) Storage -20 C for 24 months 23 μl 100 μl 100 μl Features 1. Cloning efficiency greater than 90% 2. IPTG and X-Gal are not required 3. Accepts a wide range of insert/vector ratios 0.5:1 to 12:1 4. Accepts insert size from 6 bp to 11 kb 5. The phosphorylation of PCR fragments is not required 6. Accepts blunt end amplicon or DNA fragment (not for sticky ends) 7. Resistance to ampicillin and kanamycin
Description The GetClone PCR Cloning Vector II is a positive selection system for high efficiency cloning of blunt end DNA or PCR products amplified by high fidelity DNA polymerase. The linearized GetClone pget II Vector contains a lethal gene which can be disrupted by ligation of a blunt end DNA insert into the cloning site. After ligation and transformation, only E.coli clones carrying the pget II Vector with inserted DNA at cloning site are able to propagate LB-ampicillin or LB-Kanamycin agar plates, eliminating the additional needs of IPTG and X-Gal for blue/white screening. The GetClone pget II Vector includes ampicillin and kanamycin resistance genes that can meet the needs of most users. Primers Sequence pget-for Primer: 5'-TCGAAGTTAAAGATGATTACGG-3' pget-rev Primer: 5'-TCTCTCGATAGCATTTCCTGC-3'
Ligation Example 1 (NEB T4 DNA Ligase #M0202) Insert (Blunt end) X μl (Y ng*) pget II (3954 bp) 1 μl (25 ng) Mix well then add 10X T4 DNA Ligase Buffer 2 μl T4 DNA Ligase 1 μl ddh2o to 20 μl Final volume 20 μl Mix well then incubate at 16 C or room temperature (20~25 C) for 1 hours. Ligation Example 2 (TOYOBO Ligation High ver2 #LGK-201) Insert (Blunt end) X μl (Y ng*) pget II (3954 bp) 1 μl (25 ng) ddh2o up to 7 μl Ligation high ver2 3.5 μl Final volume 10.5 μl Mix well then incubate at 16 C or room temperature (20~25 C) for 5~30 mins. *For 3/1 of Insert/Vector molar ratio:
Transformation The GetClone is compatible with most available competent E. coli cells. Apply 1 ~10 µl of ligation mixture to 10 times volume competent E. coli cells. Perform transformation procedures according to the instruction of the competent cells. Spread the transformed E. coli cells on an LB-ampicillin (50~100 µg/ml) or LB-Kanamycin (50 µg/ml) plate for colony selection. Recommended colony PCR condition (SMOBIO s TP1200 ExcelTaq 5X PCR Master Dye Mix is suggested) Template Single colony Forward primer 0.1 0.5 µm Reverse primer 0.1 0.5 µm 5X PCR Master Dye Mix 5 µl ddh 2O Variable Total volume 25 µl 94 C 2 min 94 C 30 sec 50 C 30 sec 72 C 30 sec/kb 72 C 1 min 30~35 cycles Note: The amplicon size of the colony PCR is insert size +152 bp when using pget-for Primer and pget-rev Primer.
The plasmid map and cloning sites of pget II Vector
Genetic elements of pget II Vector Element Function Position (bp) Lethal gene For screening against selfligation 1...834 MCS Multiple cloning site 278...412 Insertion site The ligation site of blunt end 354...355 insert puc-ori Initiation of replication 1022...1610 Kan R Kanamycin resistance gene 1934~2738 P1 The promoter for Kanamycin 2729-2866 resistance P2 The promoter for expressing 2970...3073 the ampicillin resistance and lethal gene Amp R Ampicillin resistance gene 3074...3953 Primer position pget-for primer Sequencing of insert, colony 284-305 PCR pget-rev primer Sequencing of insert, colony PCR 415-435
The restriction enzyme with one or two restriction sites on pget II Vector Enzyme Positions Enzyme Positions AclI 3261, 3634 MscI 2518 ApaLI 1353, 3191 NaeI 2098 BamHI 279, 375 NarI 2598, 2846 BanII 2239 NcoI 2164 BglII 434 NgoMIV 2096 BsaBI 2741,2765 PciI 1667, 3954 BspHI 947, 3023 PstI 418 BspMI 2328(c), 2709 PvuI 3494 BssHII 2199 RsrII 2081 BtgI 2164 ScaI 3382 EagI 2690 SnaBI 368 EcoRI 315 SpeI 322 FspI 2498,3640 SphI 2199 HincII 568 822 SspI 3058 HindIII 204 TatI 3380 HpaI 568, 822 For more details of the sequence of the GetClone vector, visit our website www.smobio.com
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